Evidence map›Paper›PMID 21948988›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Modeling of influenza-specific CD8+ T cells during the primary response indicates that the spleen is a major source of effectors.

Hulin Wu, Arun Kumar, Hongyu Miao, Jeanne Holden-Wiltse, Timothy R Mosmann, Alexandra M Livingstone, Gabrielle T Belz, Alan S Perelson, Martin S Zand, David J Topham

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Immunity to Influenza Infection in Humans.Cold Spring Harbor perspectives in medicine · 2021
    Review
  10. Quantifying the limits of CAR T-cell delivery in mice and men.Journal of the Royal Society, Interface · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Parameter Estimation for Semiparametric Ordinary Differential Equation Models.Communications in statistics: theory and methods · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 2 countries.

Hulin WuDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Arun Kumar
Hongyu Miao
Jeanne Holden-Wiltse
Timothy R Mosmann
Alexandra M Livingstone
Gabrielle T Belz
Alan S Perelson
Martin S Zand
David J Topham
University of Rochester Medical Center · US

Funding

Modeling B Cell Vaccine Responses in Transplant RecipientsR01AI069351 · NIAID · UNIVERSITY OF ROCHESTER · PI HYRIEN, OLLIVIER, ZAND, MARTIN S · 2007 to 2016
$3.7M
NIAID NIH HHS HHSN272201000055CNIAID NIH HHS R01 AI069351
6 · The paper itself

Abstract

The biological parameters that determine the distribution of virus-specific CD8(+) T cells during influenza infection are not all directly measurable by experimental techniques but can be inferred through mathematical modeling. Mechanistic and semimechanistic ordinary differential equations were developed to describe the expansion, trafficking, and disappearance of activated virus-specific CD8(+) T cells in lymph nodes, spleens, and lungs of mice during primary influenza A infection. An intensive sampling of virus-specific CD8(+) T cells from these three compartments was used to inform the models. Rigorous statistical fitting of the models to the experimental data allowed estimation of important biological parameters. Although the draining lymph node is the first tissue in which Ag-specific CD8(+) T cells are detected, it was found that the spleen contributes the greatest number of effector CD8(+) T cells to the lung, with rates of expansion and migration that exceeded those of the draining lymph node. In addition, models that were based on the number and kinetics of professional APCs fit the data better than those based on viral load, suggesting that the immune response is limited by Ag presentation rather than the amount of virus. Modeling also suggests that loss of effector T cells from the lung is significant and time dependent, increasing toward the end of the acute response. Together, these efforts provide a better understanding of the primary CD8(+) T cell response to influenza infection, changing the view that the spleen plays a minor role in the primary immune response.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell MovementDisease Models, AnimalFemaleInfluenza A Virus, H3N2 SubtypeLungLymph NodesLymphocyte ActivationMiceMice, Inbred C57BLModels, ImmunologicalOrthomyxoviridae InfectionsSpleen

Identifiers

PMID21948988
PMCPMC3197949
OpenAlexW2171246332

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.